Diagnostic value of salivary cortisol in end stage renal disease

• Published in: Steroids Vol. 73; no. 1; pp. 77 - 82
• Main Authors: Arregger, Alejandro L., Cardoso, Estela M.L., Tumilasci, Omar, Contreras, Liliana N.
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 2008; Elsevier Science
• Subjects: Adrenal Insufficiency - blood; Adrenal Insufficiency - diagnosis; Adrenal Insufficiency - metabolism; Adrenocorticotropic Hormone - blood; Adrenocorticotropic Hormone - pharmacology; Aldosterone - metabolism; Biological and medical sciences; Biomarkers - blood; Biomarkers - metabolism; End stage renal disease; Fundamental and applied biological sciences. Psychology; Humans; Hydrocortisone - blood; Hydrocortisone - metabolism; Hypotension; Kidney Failure, Chronic - blood; Kidney Failure, Chronic - diagnosis; Kidney Failure, Chronic - metabolism; Predictive Value of Tests; Saliva - drug effects; Saliva - metabolism; Salivary aldosterone; Salivary cortisol; Sensitivity and Specificity; Vertebrates: endocrinology; End stage renal disease; Salivary cortisol; Salivary aldosterone; Hypotension; Kidney disease; Corticosteroid; Urinary system disease; Steroid hormone; Mineralocorticoid; Terminal stage; Aldosterone; Hydrocortisone; Glucocorticoid; Nephropathy; Adrenal hormone
• ISSN: 0039-128X; 1878-5867
• DOI: 10.1016/j.steroids.2007.09.001

Salivary cortisol has been proposed a surrogate marker for free serum cortisol measurements. The aim of this study was to ascertain the diagnostic value of basal and stimulated salivary cortisol for the detection of adrenal insufficiency (AI) in hypotensive end stage renal disease (ESRD) patients. Basal salivary cortisol and basal total serum cortisol were studied in order to determine the accuracy of both biomarkers in predicting AI.
Twenty-nine ESRD patients with sustained hypotension were investigated for possible AI. Salivary cortisol was assessed at baseline and 30
min after 25
μg ACTH i.m. (LDTs). The dosage of salivary aldosterone was performed in salivary cortisol hypo-responders. Basal blood samples were drawn for steroids, renin and ACTH measurements.
A clear separation between patients with normal and impaired adrenal function was obtained through salivary cortisol levels at 30
min after ACTH. AI was detected in six cases (21%) through impaired salivary cortisol responses; stimulated salivary aldosterone helped to differentiate primary (
n
=
3) from secondary AI (
n
=
3). ROC curves showed that cutoff values for basal SAF ≤4.4
nM and serum cortisol ≤232.0
nM suggest AI (sensitivities: 93% and 69%; specificities: 86.4% and 91%, respectively).
We conclude that ACTH stimulated SAF is an accurate biomarker for the diagnosis of AI in hypotensive ESRD patients. Neither basal salivary cortisol nor serum cortisol showed 100% sensitivities for the detection of AI.